TECHNICAL FIELD
[0001] The present invention relates to an embossed thermoplastic resin sheet that is capable
of enhancing deaeration during production of laminated glass and suppressing optical
distortion of the resulting laminated glass to improve the visibility when used as
an interlayer film for laminated glass. The present invention also relates to an engraved
roll used for production of the embossed thermoplastic resin sheet, a production method
of the engraved roll, an interlayer film for laminated glass including the embossed
thermoplastic resin sheet, and a laminated glass.
BACKGROUND ART
[0002] Embossed thermoplastic resin sheets in which a large number of minute projections
and recesses (embossment) are formed on surfaces of thermoplastic resin sheets are
widely used as interlayer films for laminated glass and for other applications. For
example, a large number of minute projections and recesses are formed on a surface
of an interlayer film for laminated glass for the purpose of preventing blocking between
films, improving handleability thereof upon stacking of a glass sheet and the interlayer
film (slipperiness between the film and a glass sheet), and enhancing deaeration upon
lamination of the film and the glass sheet. Particularly, in a case where the recesses
among the recesses and the projections have a groove shape with a continuous bottom
(hereafter, also referred to as "recesses in the shape of engraved lines") and are
regularly arranged side by side in parallel with one another, such a sheet can exhibit
significantly excellent deaeration properties (see Patent Literature 1, for example).
[0003] However, use of such an embossed thermoplastic resin sheet as an interlayer film
for laminated glass causes optical distortion in the resulting laminated glass, resulting
in poor visibility.
[0004] Even in the case of a thermoplastic resin sheet on which recesses in the shape of
engraved lines are regularly arranged in parallel with one another, the sheet used
as an interlayer film for laminated glass may fail to exhibit its deaeration properties
sufficiently depending on the shape of the surface or conditions for lamination of
the sheet with a glass sheet during production of laminated glass.
CITATION LIST
- Patent Literature
SUMMARY OF INVENTION
- Technical Problem
[0006] In consideration of the state of the art, the present invention aims to provide an
embossed thermoplastic resin sheet that is capable of enhancing deaeration during
production of laminated glass and suppressing optical distortion of the resulting
laminated glass to improve the visibility when used as an interlayer film for laminated
glass, an engraved roll used for production of the embossed thermoplastic resin sheet,
a production method of the engraved roll, an interlayer film for laminated glass including
the embossed thermoplastic resin sheet, and a laminated glass.
- Solution to problem
[0007] The present invention relates to an embossed thermoplastic resin sheet having a large
number of recesses and a large number of projections on at least one surface, the
recesses each having a groove shape with a continuous bottom and being regularly arranged
side by side in parallel with one another, the thermoplastic resin sheet having not
more than three defects of the projections per mm
2 on the surface.
[0008] The present invention is specifically described in the following.
[0009] The embossed thermoplastic resin sheet of the present invention has a large number
of recesses and a large number of projections on at least one surface. The recesses
have a groove shape with a continuous bottom (recesses in the shape of engraved lines)
and are regularly arranged side by side in parallel with one another. Such a surface
shape enables the embossed thermoplastic resin sheet of the present invention to ensure
deaeration properties during production of laminated glass when used as an interlayer
film for laminated glass.
[0010] The large number of recesses and the large number of projections may be formed only
on one surface but preferably on both surfaces of the embossed thermoplastic resin
sheet as deaeration properties are significantly improved.
[0011] In the embossed thermoplastic resin sheet of the present invention, the thermoplastic
resin sheet having not more than three defects of the projections per mm
2 on the surface.
[0012] The present inventors found out that, when an embossed thermoplastic resin sheet
with many defects of projections is used as an interlayer film for laminated glass
in production of laminated glass, optical distortion may occur due to local variation
of the film thickness to possibly lower the visibility of the resulting laminated
glass. Especially in a case where the interlayer film for laminated glass has a multilayer
structure, unevenness due to the variation of the film thickness is transferred to
each interface between the layers in the interlayer film to create distortion of the
interface, which may result in more apparent optical distortion. The present inventors
also found out that defects of the projections present on the surface may block the
passage of gas during production of laminated glass, lowering the deaeration properties.
[0013] When the thermoplastic resin sheet are controlled to have not more than three defects
of the projections per mm
2 on the surface, the optical distortion of laminated glass can be suppressed to improve
the visibility of the laminated glass, while enhancing deaeration during production
of the laminated glass. The thermoplastic resin sheet has more preferably not more
than one defect, still more preferably not more than 0.5 defects, particularly preferably
not more than 0.1 defects, most preferably not more than 0.08 defects of the projections
per mm
2 on the surface. The lower limit of the number of defects of the projections is not
particularly limited. Practically, the thermoplastic resin sheet has 0.0001 defects
of the projections per mm
2 on the surface.
[0014] In a case where a thermoplastic resin sheet is not produced through a step of forming
projections and recesses using an engraved roll that is prepared by a blasting method,
such as a thermoplastic resin sheet having projections and recesses formed using an
engraved roll that is not prepared by a blasting method and a thermoplastic resin
sheet having projections and recesses formed only by control of melt fracture, the
thermoplastic resin sheet is considered to have zero defects of the projections per
mm
2 on the surface.
[0015] The number of defects of the projections in the pattern of projections and recesses
on the embossed thermoplastic resin sheet per unit area can be determined as follows.
Specifically, the surface roughness of the embossed thermoplastic resin sheet is measured
with a three-dimensional profilometer (e.g., "KS-1100" produced by KEYENCE CORPORATION,
head: model "LT-9510VM") in a 5 mm × 5 mm field of view. In the obtained image data,
Ra of the apex portions of the projections and a height difference r are measured
in a direction in parallel with the projections. The number of portions where r is
higher than Ra by 30 µm or more is counted as defects. Here, Ra refers to the arithmetic
mean roughness Ra specified in JIS B-0601 (1994). Ra is a value calculated using "KS-Analyzer
Ver. 2.00", analysis software included with the three-dimensional profilometer, in
the line roughness measurement mode based on the roughness profile data obtained by
drawing a measuring line from one end to the other end of the field of view in a direction
in parallel with the direction in which the apex portions of the projections are continuous.
The height difference r is determined as follows. The obtained roughness profile is
divided at 500-µm intervals into plural sections starting from the upper side or the
left side of the field of view with which an apex portion of a projection is in contact.
The difference between the maximum height and the minimum height in each section is
taken as the height difference r. The height difference of all the projections present
in the field of view is determined by the same method. The correction conditions employed
for obtaining the roughness profile data are cut-off value of 2.5 mm, no height smoothing,
no tilt correction, and automatic range setting. The measurement conditions other
than the field of view are as follows: stage feed condition: continuous; scan direction:
bi-directional scanning; leading axis: X axis; stage travel rate: 250.0 µm/s; axis
feed rate: 10000.0 µm/s; measuring pitch of X axis: 2.0 µm; and measuring pitch of
Y axis: 2.0 µm. By the method described above, the number of defects is counted at
at least 10 arbitrary sites, and the arithmetic mean of the obtained numbers is taken
as the average value. Especially, the arithmetic mean is preferably obtained by preparing
a roll of the resulting thermoplastic resin sheet and counting the number of defects
at at least three points on each of the positions at 1/4, 2/4, and 3/4 of the roll
from both ends in the width direction. The apex portion in this case refers to a range
corresponding to 10% of the length of a shortest straight line connecting the deepest
bottoms of two adjacent recesses in the field of view, centered on the middle of the
straight line connecting the deepest bottoms.
[0016] Ra of the apex portions of the projections is preferably 4.5 µm or less. When Ra
of the apex portions of the projections is 4.5 µm or less, excellent deaeration properties
can be exhibited in production of laminated glass.
[0017] Ra of the apex portions of the projections is preferably 1.0 µm or more. When Ra
of the apex portions of the projections is 1.0 µm or more, blocking of interlayer
films for laminated glass when they are stored in a stack can be suppressed.
[0018] The recesses in the shape of engraved lines have a roughness Rz of preferably 10
µm or more and 60 µm or less. When the roughness Rz of the recesses in the shape of
engraved lines is within the above range, further excellent deaeration properties
can be exhibited. The roughness Rz of the recesses in the shape of engraved lines
is more preferably 45 µm or less, still more preferably 40 µm or less, and more preferably
15 µm or more, still more preferably 20 µm or more.
[0019] As used herein, the roughness (Rz) of the recesses in the shape of engraved lines
is Rz specified in JIS B-0601 (1994). The roughness (Rz) can be obtained by measuring
perpendicularly so as to traverse the direction in which the recesses in the shape
of engraved lines are continuous. The measurement device may be, for example, "Surfcorder
SE300" produced by Kosaka Laboratory Ltd. The measurement may be performed at a cut-off
value of 2.5 mm, a standard length of 2.5 mm, a measurement length of 12.5 mm, a spare
length of 2.5 mm, and a stylus feed rate of 0.5 mm/sec, with a stylus having a tip
radius of 2 µm and a tip angle of 60°. The measurement is performed at 23°C and 30
RH%.
[0020] Any thermoplastic resin sheet may be used as a raw material of the embossed thermoplastic
resin sheet of the present invention, and examples thereof include a thermoplastic
resin sheet containing a polyvinyl acetal resin and a plasticizer.
[0021] The embossed thermoplastic resin sheet of the present invention can be produced by
passing a thermoplastic resin sheet as a raw material between engraved rolls, while
being heated, so that an uneven pattern on the engraved rolls is transferred to the
thermoplastic resin sheet.
[0022] The engraved rolls are commonly prepared by forming an uneven pattern on the surface
of a metal roll by a treatment such as carving or pressing of a engraving mill (mother
mill) preliminary subjected to carving to a metal roll for transferring a pattern
on the engraving mill. Moreover, a blast material may be sprayed to the surface of
the engraved roll with an aim of concurrently forming a pattern of minute projections
and minute recesses in addition to the pattern of projections and recesses formed
by engraving.
[0023] As a result of intensive studies, the present inventors found out that defects of
the projections present on the surface of an embossed thermoplastic resin sheet are
caused by defective transfer in which an uneven pattern is not accurately transferred
upon transferring of the pattern from an engraved roll. The present inventors also
found out that such defective transfer is caused by blast material pieces remaining
in recessed grooves on the engraved roll. In the blasting method, an uneven pattern
is formed by spraying a blast material to the surface of a raw material roll while
rotating the raw material roll. In a case where the engraved roll has recessed grooves
and the recessed grooves have an acute bottom or a very narrow flat bottom, the blast
material may clog and remain in the recessed grooves during the above treatment. When
an embossed thermoplastic resin sheet is produced using such an engraved roll with
the blast material remaining thereon, the shape of the blast material may be transferred
to the projections of the embossed thermoplastic resin sheet which are formed in correspondence
with the recessed grooves on the engraved roll. Accordingly, the projections are deformed
to have abnormal projections and recesses on the apex portions.
[0024] The present inventors made further intensive studies to find out that, even in the
case of production by the blasting method, the use of an engraved roll having, per
unit area on average, not more than three blast material pieces with a maximum length
of 10 µm or more in the grooves per mm
2 of the engraved roll enables significant reduction of occurrence of defective transfer,
resulting in production of the embossed thermoplastic resin sheet of the present invention
having not more than three defects of the projections per mm
2 on the surface.
[0025] The present invention also encompasses an engraved roll formed by a blasting method,
the engraved roll having an uneven pattern including recessed grooves arranged in
parallel with one another in the circumferential direction, the engraved roll having,
per unit area on average, not more than three pieces of a blast material with a maximum
length of 10 µm or in the recessed grooves per mm
2 of the engraved roll.
[0026] The engraved roll of the present invention is made of a metal such as iron, carbon
steel, alloyed steel, nickel-chromium steel, or chromium steel. For excellent durability,
the engraved roll is preferably made of carbon steel or alloyed steel.
[0027] The engraved roll of the present invention has an uneven pattern including recessed
grooves arranged on the surface in parallel with one another in the circumferential
direction. The use of such an engraved roll enables production of an embossed thermoplastic
resin sheet. The engraved roll of the present invention preferably has an uneven pattern
including projected ridges and recessed grooves arranged on the surface in parallel
with one another in the circumferential direction.
[0028] The pattern of projections and recesses on the engraved roll of the present invention
needs to provide an interlayer film for laminated glass (embossed thermoplastic resin
sheet) with a pattern that exhibits favorable slipperiness with a glass surface when
the interlayer film is tightly attached to a glass sheet and facilitates deaeration
between the glass surface and the interlayer film. For the above purpose, the pattern
of projections and recesses includes recessed grooves formed in parallel with one
another in the circumferential direction of the engraved roll. In the case where projected
ridges and recessed grooves are formed in parallel with one another on the surface
in the circumferential direction of the engraved roll, the projected ridges may be
formed in the shape of a lattice for the purpose of improving the adhesiveness to
glass. The width and height of projected ridges and the intervals between the projected
ridges may be determined as appropriate for adjusting deaeration properties and self-adhesiveness.
[0029] The state "recessed grooves are formed in parallel with one another in the circumferential
direction" refers not only to a case where recessed grooves are formed in a direction
completely in parallel with the circumferential direction, i.e., a direction perpendicular
to the rotation axis of the engraved roll, but also to a case where recessed grooves
are formed in parallel with one another at a predetermined angle relative to the circumferential
direction.
[0030] The engraved roll of the present invention has, per unit area on average, not more
than three blast material pieces with a maximum length of 10 um or more in the recessed
grooves per mm
2 of the engraved roll. Such an engraved roll enables production of an embossed thermoplastic
resin sheet having an uneven pattern accurately transferred thereon with few defects,
significantly reducing occurrence of defective transfer. The engraved roll has, per
unit area on average, preferably not more than two blast material pieces, more preferably
not more than one blast material piece with a maximum length of 10 µm or more in the
recessed grooves per mm
2 of the engraved roll. The lower limit of the number of blast material pieces with
a maximum length of 10 µm or more in the recessed grooves, per unit area on average,
is not particularly limited. Practically, the engraved roll has, per unit area on
average, 0.0001 blast material pieces with a maximum length of 10 µm or more in the
recessed grooves per mm
2 of the engraved roll. In the case of an engraved roll prepared not by a blast method,
such an engraved roll is considered to have, per unit area on average, zero blast
material pieces with a maximum length of 10 µm or more in the recessed grooves per
mm
2 of the engraved roll.
[0031] The "blast material with a maximum length of 10 µm or more" is herein counted in
consideration of the size of remaining blast material pieces that may actually cause
defective transfer. The maximum length as used herein refers to the maximum length
of a blast material observed in a recessed groove of the engraved roll with a microscope.
More specifically, the maximum length as used herein refers to the length between
two farthest points on the circumference of one blast material observed with a microscope.
[0032] The number of blast material pieces in the recessed grooves per unit area is determined
by counting the number of remaining blast material pieces with a maximum length of
10 µm or more present in a range of 1290 µm × 1024 µm in a recessed groove portion
of the engraved roll photographed at a 200x magnification with a microscope (e.g.,
"Dino-Lite Pro2, model: DILITE80" produced by AnMo Electronics corporation). The number
of remaining blast material pieces is counted by the above method at at least 30 arbitrary
sites, and the arithmetic mean of the obtained numbers is taken as the average number.
Especially, the arithmetic mean is preferably obtained by counting the number of remaining
materials at at least 10 points on each of the positions at 1/4, 2/4, and 3/4 of the
obtained engraved roll from both ends in the width direction in such a manner that
each field of view does not overlap with each other.
[0033] The engraved roll of the present invention is produced by a blasting method. The
present inventors made intensive studies to find out that when a predetermined method
for producing an engraved roll is employed, the produced engraved roll has, per unit
area on average, not more than three blast material pieces with a maximum length of
10 µm or more in the recessed grooves per mm
2 of the engraved roll.
[0034] The present invention also encompasses a method for producing an engraved roll by
a blasting method, the method including: a step of forming an uneven pattern by spraying
a blast material to a raw material roll having recessed grooves formed in parallel
with one another in the circumferential direction, the blasting material being sprayed
at an angle of 20° or smaller relative to a line connecting the tip of a blast gun
and the axis of the raw material roll while rotating the raw material roll; and a
step of removing the blast material remaining in the recessed grooves by spraying
the blast material at an angle of ±20° or smaller relative to a tangential plane direction
(tangential direction at the vertical section of the roll) of the roll and in a direction
in parallel with the recessed grooves of the roll, while rotating the roll having
the uneven pattern.
[0035] The method for producing an engraved roll of the present invention is described with
reference to Figs. 1 and 2.
[0036] The method for producing an engraved roll of the present invention first includes
a step of forming an uneven pattern by spraying a blast material to a raw material
roll having recessed grooves formed in parallel with one another in the circumferential
direction, the blast material being sprayed at an angle of 20° or smaller relative
to the line connecting the tip of a blast gun and the axis of the raw material roll
while rotating the raw material roll (Figs. 1(a), 1(b)).
[0037] In Fig. 1, a blast gun 2 sprays a blast material to a rotating roll 1. The blast
material is sprayed at an angle of 20° or smaller relative to the line connecting
the tip of the blast gun and the axis of the roll.
[0038] Any raw material roll may be used. A preferred raw material roll is a mirror-finished
iron roll on which recessed grooves are formed in parallel with one another in the
circumferential direction by milling or carving.
[0039] The recessed grooves are not limited. When the bottom of a recessed portion is wide,
the blast material is less likely to clog the groove. When the bottom has a width
of 5 µm or more, the blast material is less likely to clog the groove, though it depends
on the particle size or the kind of the blast materials. When the bottom has a width
of 15 µm or more, the blast material is further less likely to clog the groove. When
the bottom has a width of 40 µm or more, the blast material is still further less
likely to clog the groove.
[0040] When the recessed portion has a larger angle of inclination, the recessed portion
has a wider groove at a point close to the surface layer of the roll, which prevents
clogging of a shallow part of the roll with the blast materials. Accordingly, the
blast material is less likely to clog the groove. Specifically, when the angle of
inclination is 5° or more, the blast material is less likely to clog the groove. When
the angle of inclination is 15° or more, the blast material is further less likely
to clog the groove. When the angle of inclination is 30° or more, the blast material
is still further less likely to clog the groove.
[0041] The recessed groove with a greater groove height can further prevent defective transfer
to the thermoplastic resin sheet. When the groove height of the recessed groove is
150 µm or more, defective transfer to the thermoplastic resin sheet can be still further
prevented. When the groove height of the recessed groove is 250 µm or more, defective
transfer to the thermoplastic resin sheet can be furthermore prevented. When the groove
height of the recessed groove is 330 µm or more, defective transfer to the thermoplastic
resin sheet can be still furthermore prevented.
[0042] The recessed grooves are preferably formed at a larger pitch interval for the following
reason. When the pitch interval between the recessed grooves is larger, the number
of grooves per unit area is smaller. Then, even when the grooves are clogged with
the blast material, the number of blast material pieces transferred to a thermoplastic
resin sheet becomes smaller so that defective transfer can be further prevented. Specifically,
when the pitch interval between the recessed grooves is 100 µm or more, defective
transfer can be prevented. When the pitch interval between the recessed grooves is
200 µm or more, defective transfer can be further prevented. When the pitch interval
between the recessed grooves is 300 µm or more, defective transfer can be still further
prevented. The upper limit of the pitch interval between the recessed grooves is not
particularly limited, and is practically 10000 µm or less. For improvement of the
deaeration properties and reduction of the optical distortion in production of laminated
glass in a case where the thermoplastic resin sheet is used as an interlayer film
for laminated glass, the upper limit of the pitch interval is preferably 600 µm or
less, more preferably 400 µm or less, still more preferably 300 µm or less.
[0043] The axis angle of the recessed groove on the raw material roll surface is not particularly
limited, and may be appropriately determined in accordance with the properties, such
as self-adhesiveness, of the thermoplastic resin sheet.
[0044] Fig. 3 is a schematic view for explaining the groove height of a recessed portion,
the width of a bottom portion, the pitch interval, the angle of inclination, and the
axis angle of a recessed groove.
[0045] The groove height refers to a difference between the maximum height and the minimum
height in a cross-section of a raw material roll in the direction perpendicular to
the direction of grooves. The width of a bottom portion refers to a length of a region
of the minimum height. The pitch interval refers to a distance between a bisector
of the width of a bottom portion and a bisector of the width of an adjacent bottom
portion. In a case where the bottom portion has no width, the pitch interval refers
to a distance between a minimum height portion of a groove and a minimum height portion
of an adjacent groove. The angle of inclination refers to an angle formed between
a perpendicular of the roll axis and a slope from an end of a bottom portion to a
projection (Fig. 3(b)).
[0046] The axis angle of a recessed groove refers to an intersection angle between a recessed
groove on the surface of the raw material roll and the rotation axis of the roll (Fig.
3(a)).
[0047] The blast material used may be metallic particles made of cast iron, cast steel,
or the like, or non-metallic particles made of silica sand, glass, garnet, silicon,
aluminum oxide (alumina), or the like. The blast material used may be in the form
of shots, grits, beads, cut wires, or the like. Particularly preferred is a blast
material made of aluminum oxide in the form of grits.
[0048] The blast material is preferably a blast material with a grit size in a range of
#240 to #1200, more preferably a blast material with a grit size in a range of #280
to #800 specified in the JIS standard (JIS R 6001-1998).
[0049] The conditions for spraying a blast material in the step of forming projections and
recesses, the rotation speed of a raw material roll, or the like may be the same as
those employed in a production method of an engraved roll by a common air blasting
method. For example, a blast material may be sprayed using a nozzle with an aperture
of 5 to 50 mm under the conditions of an air pressure of 1 to 12 kgf/cm
2, the number of passes of 1 to 5 times, a nozzle feed rate of 0.1 to 50 mm/rotation,
and a rotation speed of a raw material roll at 1 to 40 m/min.
[0050] The nozzle may have a polygonal, perfect circle, or elliptical mouth, and preferably
has a perfect circle mouth. The aperture of the nozzle refers to the maximum width
of the nozzle mouth.
[0051] The blast material may be spouted out by direct pressure blasting, suction blasting,
blasting by a blower, or the like. Preferred among these is direct pressure blasting.
[0052] In the step of forming projections and recesses, a blast material is sprayed at an
angle of 20° or smaller relative to the line connecting the tip of a blast gun and
the axis of a raw material roll. This enables efficient formation of an uneven pattern
on the surface of a raw material roll. The angle is preferably 10° or smaller, more
preferably 5° or smaller.
[0053] The method for producing an engraved roll of the present invention next includes
a step of removing the blast material remaining in the recessed grooves by spraying
the blast material at an angle of ±20° or smaller relative to the tangential plane
direction of the roll and in a direction in parallel with the recessed grooves formed
on the roll, while rotating the roll having the uneven pattern (Figs. 2(a), 2(b)).
[0054] By spraying the blast material at an angle of ±20° or smaller relative to the tangential
plane direction of the roll and in the direction in parallel with the recessed grooves
in the pattern of projections and recessed formed on the roll, the blast material
clogging the recessed grooves in the step of forming projections and recesses can
be blown away to be removed. The angle is preferably ±10° or smaller, more preferably
±5° or smaller.
[0055] The conditions for spraying the blast material in the step of removing the blast
material, the rotation speed of the raw material roll, or the like may be the same
as those in the step of forming projections and recesses.
[0056] In the step of removing the blast materials, the blast material is sprayed at an
angle of ±20° or smaller relative to the tangential plane direction of the roll and
in the direction in parallel with the recessed grooves formed on the roll. This ensures
removal of blast materials.
[0057] Alternatively, the blast material may also be removed by running a brush along the
recessed grooves of the roll on which projections and recesses are formed. For more
reliable removal of the blast material remaining in the recessed grooves, more preferred
as the method employed in the step of removing the blast material is the method of
spraying the blast material at an angle of ±20° or smaller relative to the tangential
plane direction of the roll and in the direction in parallel with the recessed grooves
formed on the roll.
[0058] Use of the engraved roll of the present invention can prevent occurrence of defective
transfer to enable production of an embossed thermoplastic resin sheet in which the
number of defects of the projections on the surface is significantly small.
[0059] The present invention also encompasses an embossed thermoplastic resin sheet having
projections and recesses formed using the engraved roll of the present invention.
[0060] The embossed thermoplastic resin sheet of the present invention can be suitably used
as an interlayer film for laminated glass.
[0061] The present invention also encompasses an interlayer film for laminated glass including
the embossed thermoplastic resin sheet of the present invention.
[0062] In a case where the embossed thermoplastic resin sheet of the present invention is
used as an interlayer film for laminated glass, examples of the thermoplastic resin
include polyvinylidene fluoride, polytetrafluoroethylene, vinylidene fluoride-propylene
hexafluoride copolymers, polyethylene trifluoride, acrylonitrile-butadiene-styrene
copolymers, polyester, polyether, polyamide, polycarbonate, polyacrylate, polymethacrylate,
polyvinyl chloride, polyethylene, polypropylene, polystyrene, polyvinyl acetal, and
ethylene-vinyl acetate copolymers. Preferred among these are polyvinyl acetal or ethylene-vinyl
acetate copolymers, and more preferred is polyvinyl acetal.
[0063] The polyvinyl acetal can be produced by, for example, acetalization of a polyvinyl
alcohol with an aldehyde. The polyvinyl alcohol can be produced by, for example, saponification
of a polyvinyl acetate. The degree of saponification of the polyvinyl alcohol is usually
in the range of 70 to 99.8 mol%.
[0064] The polyvinyl alcohol preferably has an average degree of polymerization of 200 or
more, more preferably 500 or more, still more preferably 1700 or more, particularly
preferably more than 1700, and preferably 5000 or less, more preferably 4000 or less,
still more preferably 3000 or less, particularly preferably less than 3000. When the
average degree of polymerization is equal to or more than the lower limit, the laminated
glass has even higher penetration resistance. When the average degree of polymerization
is equal to or lower than the upper limit, formation of the interlayer film is facilitated.
The average degree of polymerization of the polyvinyl alcohol can be determined in
accordance with JIS K6726 "Testing methods for polyvinyl alcohol".
[0065] The acetal group contained in the polyvinyl acetal may have any number of carbons.
The polyvinyl acetal can be produced with any aldehyde. The lower limit of the carbon
number of the acetal group in the polyvinyl acetal is preferably 3, and the upper
limit thereof is preferably 6. When the acetal group in the polyvinyl acetal has a
carbon number of 3 or greater, the interlayer film has a sufficiently low glass transition
temperature. In addition, bleed-out of the plasticizer can be prevented. When the
aldehyde has a carbon number of 6 or less, polyvinyl acetal can be easily synthesized,
ensuring the productivity. The C3-C6 aldehyde may be a linear aldehyde or a branched
aldehyde. Examples thereof include n-butylaldehyde and n-valeraldehyde
[0066] The aldehyde is not limited. Commonly, a C1-C10 aldehyde is preferably used. Examples
of such a C1-C10 aldehyde include propionaldehyde, n-butyraldehyde, isobutyraldehyde,
n-valeraldehyde, 2-ethylbutyraldehyde, n-hexylaldehyde, n-octylaldehyde, n-nonylaldehyde,
n-decylaldehyde, formaldehyde, acetaldehyde, and benzaldehyde. In particular, preferred
are propionaldehyde, n-butyraldehyde, isobutyraldehyde, n-hexylaldehyde, and n-valeraldehyde.
More preferred are propionaldehyde, n-butyraldehyde, and isobutyraldehyde. Still more
preferred is n-butyraldehyde. These aldehydes may be used alone or in combination
of two or more.
[0067] The polyvinyl acetal preferably has a hydroxy group content (amount of hydroxy groups)
of 10 mol% or more, more preferably 15 mol% or more, still more preferably 18 mol%
or more, and preferably 40 mol% or less, more preferably 35 mol% or less. When the
hydroxy group content is equal to or more than the lower limit, the interlayer film
has even higher adhesiveness. When the hydroxy group content is equal to or less than
the upper limit, the interlayer film has high flexibility, making it easy to handle
the interlayer film. The hydroxy group content of the polyvinyl acetal herein means
a mole fraction expressed in percentage, determined by dividing the amount of ethylene
groups to which hydroxy groups are bonded by the amount of all the ethylene groups
in the main chain. The amount of ethylene groups to which hydroxy groups are bonded
may be determined, for example, in accordance with JIS K6726 "Testing methods for
polyvinyl alcohol" or ASTM D1396-92.
[0068] The degree of acetylation (acetyl group content) of the polyvinyl acetal is preferably
0.1 mol% or more, more preferably 0.3 mol% or more, still more preferably 0.5 mol%
or more, and preferably 30 mol% or less, more preferably 25 mol% or less, still more
preferably 20 mol% or less. When the degree of acetylation is equal to or more than
the lower limit, the polyvinyl acetal has higher compatibility with a plasticizer.
When the degree of acetylation is equal to or less than the upper limit, the interlayer
film and the laminated glass have higher moisture resistance. The degree of acetylation
herein means the mole fraction expressed in percentage, determined by subtracting
the amount of ethylene groups to which acetal groups are bonded and the amount of
ethylene groups to which hydroxy groups are bonded from the amount of all the ethylene
groups in the main chain and dividing the resulting value by the amount of all the
ethylene groups in the main chain. The amount of ethylene groups to which acetal groups
are bonded can be determined, for example, in accordance with JIS K 6728 "Testing
methods for polyvinyl butyral" or ASTM D1396-92.
[0069] The degree of acetalization of the polyvinyl acetal (degree of butyralization, in
the case of the polyvinyl butyral resin) is preferably 50 mol% or more, more preferably
53 mol% or more, still more preferably 60 mol% or more, particularly preferably 63
mol% or more, and preferably 85 mol% or less, more preferably 75 mol% or less, still
more preferably 70 mol% or less. When the degree of acetalization is equal to or more
than the lower limit, the polyvinyl acetal has higher compatibility with a plasticizer.
When the degree of acetalization is equal to or less than the upper limit, the production
of the polyvinyl acetal requires less reaction time. The degree of acetalization herein
means the mole fraction expressed in percentage, determined by dividing the amount
of ethylene groups to which acetal groups are bonded by the amount of all the ethylene
groups in the main chain. The degree of acetalization can be calculated by measuring
the degree of acetylation and the hydroxy group content in accordance with JIS K6728
"Testing methods for polyvinyl butyral" or ASTM D1396-92, calculating the mole fraction
from the measurements, and then subtracting the degree of acetylation and the hydroxy
group content from 100 mol%.
[0070] The hydroxy group content (amount of hydroxy groups), the degree of acetalization
(degree of butyralization), and the degree of acetylation are preferably calculated
based on the results of the measurement by a method in conformity with JIS K6728 "Testing
methods for polyvinyl butyral" . In a case where polyvinyl acetal is a polyvinyl butyral
resin, the hydroxy group content (amount of hydroxy groups), degree of acetalization
(degree of butyralization), and the degree of acetylation are preferably calculated
based on the results of the measurement by a method in conformity with JIS K6728 "Testing
methods for polyvinyl butyral".
[0071] The interlayer film for laminated glass of the present invention preferably contains
a plasticizer.
[0072] Any plasticizer commonly used for an interlayer film for laminated glass can be used.
Examples thereof include organic plasticizers such as monobasic organic acid esters
or polybasic organic acid esters, and phosphoric acid plasticizers such as organophosphate
compounds or organophosphite compounds.
[0073] Examples of the organic plasticizers include triethylene glycol-di-2-ethylhexanoate,
triethylene glycol-di-2-ethylbutyrate, triethylene glycol-di-n-heptanoate, tetraethylene
glycol-di-2-ethylhexanoate, tetraethylene glycol-di-2-ethyl butyrate, tetraethylene
glycol-di-n-heptanoate, diethylene glycol-di-2-ethylhexanoate, diethylene glycol-di-2-ethylbutyrate,
and diethylene glycol-di-n-heptanoate. In particular, the interlayer film preferably
contains triethylene glycol-di-2-ethylhexanoate, triethylene glycol-di-2-ethylbutyrate,
or triethylene glycol-di-n-heptanoate, more preferably contains triethylene glycol-di-2-ethylhexanoate.
[0074] The amount of the plasticizer is not limited. The amount of the plasticizer based
on 100 parts by mass of the thermoplastic resin is preferably 25 parts by mass or
more, more preferably 30 parts by mass or more, and preferably 80 parts by mass or
less, more preferably 70 parts by mass or less. When the plasticizer content is equal
to or more than the lower limit, the laminated glass can have even higher penetration
resistance. When the plasticizer content is equal to or lower than the upper limit,
the interlayer film has even higher transparency.
[0075] The interlayer film for laminated glass of the present invention preferably contains
an adhesion modifier.
[0076] The adhesion modifier is preferably, for example, an alkali metal salt or an alkaline
earth metal salt. Examples of the adhesion modifier include salts such as potassium,
sodium, or magnesium salt. Examples of the acid constituting the salts include carboxylic
organic acids such as octylic acid, hexylic acid, 2-ethylbutyric acid, butyric acid,
acetic acid, and formic acid and inorganic acids such as hydrochloric acid and nitric
acid. Preferred among these is magnesium salt because adhesiveness between glass and
the interlayer film for laminated glass can be easily adjusted.
[0077] In a case where the interlayer film for laminated glass of the present invention
includes a laminate of two or more resin layers, the adhesion modifier is preferably
contained at least in a resin layer that is to be in contact with glass.
[0078] The interlayer film for laminated glass of the present invention may optionally contain
additives such as an antioxidant, a light stabilizer, modified silicone oil as an
adhesion modifier, a flame retardant, an antistatic agent, a moisture-proof agent,
a heat reflecting agent, or a heat absorbing agent.
[0079] The interlayer film for laminated glass of the present invention includes at least
a first resin layer and a second resin layer as two or more resin layers. The hydroxy
group content of polyvinyl acetal (hereafter, referred to as polyvinyl acetal A) in
the first resin layer is preferably different from the hydroxy group content of polyvinyl
acetal (hereafter, referred to as polyvinyl acetal B) in the second resin layer. Since
the polyvinyl acetal A and the polyvinyl acetal B have different properties, various
properties that cannot be achieved by a monolayer structure can be imparted to the
interlayer film for laminated glass. For example, in a case where the first resin
layer is interposed between two second resin layers and the hydroxy group content
of the polyvinyl acetal A is smaller than the hydroxy group content of the polyvinyl
acetal B, the first resin layer tends to have a lower glass transition temperature
than the second resin layer. As a result, the first resin layer is softer than the
second resin layer, so that the interlayer film for laminated glass has better sound-insulating
properties. For another example, in a case where the first resin layer is interposed
between two second resin layers and the hydroxy group content of the polyvinyl acetal
A is greater than the hydroxy group content of the polyvinyl acetal B, the first resin
layer tends to have a higher glass transition temperature than the second resin layer.
As a result, the first resin layer is harder than the second resin layer, so that
the interlayer film for laminated glass has better penetration resistance.
[0080] Moreover, in a case where the first resin layer and the second resin layer contain
a plasticizer, the plasticizer content (hereafter, referred to as content A) in the
first resin layer based on 100 parts by mass of polyvinyl acetal is preferably different
from the plasticizer content (hereafter, referred to as content B) in the second resin
layer based on 100 parts by mass of polyvinyl acetal. For example, in a case where
the first resin layer is interposed between two second resin layers and the content
A is greater than the content B, the first resin layer tends to have a lower glass
transition temperature than the second resin layer. As a result, the first resin layer
is softer than the second resin layer, so that the interlayer film for laminated glass
has better sound-insulating properties. In a case where the first resin layer is interposed
between two second resin layers and the content A is smaller than the content B, the
first resin layer tends to have a higher glass transition temperature than the second
resin layer. As a result, the first resin layer is harder than the second resin layer,
so that the interlayer film for laminated glass has better penetration resistance.
[0081] An exemplary combination of two or more resin layers included in the interlayer film
for laminated glass of the present invention includes a sound insulation layer as
the first resin layer and a protective layer as the second resin layer with an aim
of improving the sound-insulating properties of the laminated glass. Preferably, the
sound insulation layer contains polyvinyl acetal X and a plasticizer and the protective
layer contains polyvinyl acetal Y and a plasticizer because the laminated glass can
have better sound-insulating properties. Moreover, in a case where the sound insulation
layer is interposed between two protective layers, an interlayer film for laminated
glass excellent in sound-insulating properties (hereafter, also referred to as a sound-insulating
interlayer film) can be obtained. Hereafter, a sound-insulating interlayer film is
more specifically described.
[0082] In the sound-insulating interlayer film, the sound insulation layer has a function
of imparting sound-insulating properties. The sound insulation layer preferably contains
polyvinyl acetal X and a plasticizer. The polyvinyl acetal X can be prepared by acetalization
of polyvinyl alcohol with an aldehyde. Commonly, the polyvinyl alcohol can be obtained
by saponification of polyvinyl acetate. The lower limit of the average degree of polymerization
of the polyvinyl alcohol is preferably 200, whereas the upper limit thereof is preferably
5000. When the average degree of polymerization of the polyvinyl alcohol is 200 or
higher, the penetration resistance of the sound-insulating interlayer film to be obtained
can be improved. When the average degree of polymerization of the polyvinyl alcohol
is 5000 or lower, formability of the sound insulation layer can be ensured. The lower
limit of the average degree of polymerization of the polyvinyl alcohol is more preferably
500, whereas the upper limit thereof is more preferably 4000. The average degree of
polymerization of the polyvinyl alcohol is determined in accordance with JIS K6726
"Testing methods for polyvinyl alcohol".
[0083] The lower limit of the carbon number of an aldehyde used for acetalization of the
polyvinyl alcohol is preferably 4, whereas the upper limit thereof is preferably 6.
When the carbon number of the aldehyde is 4 or more, the sound insulation layer can
stably contain a sufficient amount of a plasticizer to exhibit excellent sound-insulating
properties. Moreover, bleed-out of the plasticizer can be prevented. When the carbon
number of the aldehyde is 6 or less, synthesis of the polyvinyl acetal X is facilitated
to ensure the productivity. The C4-C6 aldehyde may be a linear or branched aldehyde,
and examples thereof include n-butyraldehyde and n-valeraldehyde.
[0084] The upper limit of the hydroxy group content of the polyvinyl acetal X is preferably
30 mol%. When the hydroxy group content of the polyvinyl acetal X is 30 mol% or less,
the sound insulation layer can contain the plasticizer in an amount needed for exhibiting
sound-insulating properties, and bleed-out of the plasticizer can be prevented. The
upper limit of the hydroxy group content of the polyvinyl acetal X is more preferably
28 mol%, still more preferably 26 mol%, particularly preferably 24 mol%, whereas the
lower limit thereof is preferably 10 mol%, more preferably 15 mol%, still more preferably
20 mol%. The hydroxy group content of the polyvinyl acetal X is a value in percentage
(mol%) of the mole fraction obtained by dividing the amount of ethylene groups to
which hydroxy groups are bonded by the amount of all the ethylene groups in the main
chain. The amount of ethylene groups to which hydroxy groups are bonded can be obtained
by measuring the amount of ethylene groups to which hydroxy groups are bonded in the
polyvinyl acetal X in accordance with JIS K6728 "Testing methods for polyvinyl butyral".
[0085] The lower limit of the acetal group content of the polyvinyl acetal X is preferably
60 mol%, whereas the upper limit thereof is preferably 85 mol%. When the acetal group
content of the polyvinyl acetal X is 60 mol% or more, the sound insulation layer has
higher hydrophobicity and can contain a plasticizer in an amount needed for exhibiting
sound-insulating properties, and bleed-out of the plasticizer and whitening can be
prevented. When the acetal group content of the polyvinyl acetal X is 85 mol% or less,
synthesis of the polyvinyl acetal X is facilitated to ensure the productivity. The
lower limit of the acetal group content of the polyvinyl acetal X is more preferably
65 mol%, still more preferably 68 mol%. The acetal group content can be obtained by
measuring the amount of ethylene groups to which acetal groups are bonded in the polyvinyl
acetal X in accordance with JIS K6728 "Testing methods for polyvinyl butyral".
[0086] The lower limit of the acetyl group content of the polyvinyl acetal X is preferably
0.1 mol%, whereas the upper limit thereof is preferably 30 mol%. When the acetyl group
content of the polyvinyl acetal X is 0.1 mol% or more, the sound insulation layer
can contain a plasticizer in an amount needed for exhibiting sound-insulating properties,
and bleed-out can be prevented. When the acetyl group content of the polyvinyl acetal
X is 30 mol% or less, the sound insulation layer has higher hydrophobicity to prevent
whitening. The lower limit of the acetyl group content is more preferably 1 mol%,
still more preferably 5 mol%, particularly preferably 8 mol%, whereas the upper limit
thereof is more preferably 25 mol%, still more preferably 20 mol%. The acetyl group
content is a value in percentage (mol%) of the mole fraction obtained by subtracting
the amount of ethylene groups to which acetal groups are bonded and the amount of
ethylene groups to which hydroxy groups are bonded from the amount of all the ethylene
groups in the main chain and dividing the resulting value by the amount of all the
ethylene groups in the main chain.
[0087] In particular, the polyvinyl acetal X is preferably polyvinyl acetal with the acetyl
group content of 8 mol% or more or polyvinyl acetal with the acetyl group content
of less than 8 mol% and the acetal group content of 65 mol% or more because the sound
insulation layer can easily contain a plasticizer in an amount needed for exhibiting
sound-insulating properties. The polyvinyl acetal X is more preferably polyvinyl acetal
having an acetyl group content of 8 mol% or more or polyvinyl acetal having an acetyl
group content of less than 8 mol% and an acetal group content of 68 mol% or more.
[0088] The lower limit of the plasticizer content of the sound insulation layer is preferably
45 parts by mass, whereas the upper limit thereof is preferably 80 parts by mass based
on 100 parts by mass of the polyvinyl acetal X. When the plasticizer content is 45
parts by mass or more, high sound-insulating properties can be exhibited. When the
plasticizer content is 80 parts by mass or less, bleed-out of the plasticizer is prevented,
so that the transparency or adhesiveness of the interlayer film for laminated glass
is not lowered. The lower limit of the plasticizer content is more preferably 50 parts
by mass, still more preferably 55 parts by mass, whereas the upper limit thereof is
more preferably 75 parts by mass, still more preferably 70 parts by mass.
[0089] The lower limit of the thickness of the sound insulation layer is preferably 50 µm.
When the thickness of the sound insulation layer is 50 µm or more, sufficient sound-insulating
properties can be exhibited. The lower limit of the thickness of the sound insulation
layer is more preferably 80 µm. The upper limit thereof is not particularly limited,
and is preferably 300 µm in consideration of the thickness as an interlayer film for
laminated glass.
[0090] The protective layer has a function of preventing bleed-out of a large amount of
a plasticizer contained in the sound insulation layer to prevent lowering of the adhesiveness
between the interlayer film for laminated glass and glass and imparting penetration
resistance to the interlayer film for laminated glass. The protective layer preferably
contains, for example, polyvinyl acetal Y and a plasticizer, more preferably polyvinyl
acetal Y with a greater hydroxy group content than the polyvinyl acetal X and a plasticizer.
[0091] The polyvinyl acetal Y can be prepared by acetalization of polyvinyl alcohol with
an aldehyde. The polyvinyl alcohol can be commonly obtained by saponification of polyvinyl
acetate. The lower limit of the average degree of polymerization of the polyvinyl
alcohol is preferably 200, whereas the upper limit thereof is preferably 5000. When
the average degree of polymerization of the polyvinyl alcohol is 200 or more, the
penetration resistance of the interlayer film for laminated glass can be improved.
When the average degree of polymerization of the polyvinyl alcohol is 5000 or less,
the formability of the protective layer can be ensured. The lower limit of the average
degree of polymerization of the polyvinyl alcohol is more preferably 500, whereas
the upper limit thereof is more preferably 4000.
[0092] The lower limit of the carbon number of an aldehyde used for acetalization of the
polyvinyl alcohol is preferably 3, whereas the upper limit thereof is preferably 4.
When the carbon number of the aldehyde is 3 or more, the penetration resistance of
the interlayer film for laminated glass is improved. When the carbon number of the
aldehyde is 4 or less, the productivity of the polyvinyl acetal Y is improved. The
C3-C4 aldehyde may be a linear or branched aldehyde, and examples thereof include
n-butyraldehyde.
[0093] The upper limit of the hydroxy group content of the polyvinyl acetal Y is preferably
33 mol%, whereas the lower limit thereof is preferably 28 mol%. When the hydroxy group
content of the polyvinyl acetal Y is 33 mol% or less, whitening of the interlayer
film for laminated glass can be prevented. When the hydroxy group content of the polyvinyl
acetal Y is 28 mol% or more, the penetration resistance of the interlayer film for
laminated glass can be improved.
[0094] The lower limit of the acetal group content of the polyvinyl acetal Y is preferably
60 mol%, whereas the upper limit thereof is preferably 80 mol%. When the acetal group
content is 60 mol% or more, the protective layer can contain a plasticizer in an amount
needed for exhibiting sufficient penetration resistance. When the acetal group content
is 80 mol% or less, the adhesiveness between the protective layer and glass can be
ensured. The lower limit of the acetal group content is more preferably 65 mol%, whereas
the upper limit thereof is more preferably 69 mol%.
[0095] The upper limit of the acetyl group content of the polyvinyl acetal Y is preferably
7 mol%. When the acetyl group content of the polyvinyl acetal Y is 7 mol% or less,
the protective layer has higher hydrophobicity, thereby preventing whitening. The
upper limit of the acetyl group content is more preferably 2 mol%, whereas the lower
limit thereof is preferably 0.1 mol%. The hydroxy group contents, acetal group contents,
and acetyl group contents of the polyvinyl acetal A, B, and Y can be measured by the
same method as in the case of the polyvinyl acetal X.
[0096] The lower limit of the plasticizer content of the protective layer is preferably
20 parts by mass, whereas the upper limit thereof is preferably 45 parts by mass based
on 100 parts by mass of the polyvinyl acetal Y. When the plasticizer content is 20
parts by mass or more, the penetration resistance can be ensured. When the plasticizer
content is 45 parts by mass or less, bleed-out of the plasticizer can be prevented,
so that the transparency and adhesiveness of the interlayer film for laminated glass
is not lowered. The lower limit of the plasticizer content is more preferably 30 parts
by mass, still more preferably 35 parts by mass, whereas the upper limit thereof is
more preferably 43 parts by mass, still more preferably 41 parts by mass. The plasticizer
content of the protective layer is preferably smaller than the plasticizer content
of the sound insulation layer because sound-insulating properties can be further improved
in the laminated glass.
[0097] The hydroxy group content of the polyvinyl acetal Y is preferably greater than the
hydroxy group content of the polyvinyl acetal X, more preferably greater by 1 mol%
or more, still more preferably greater by 5 mol% or more, particularly preferably
greater by 8 mol% or more because the sound-insulating properties of the laminated
glass is further improved. Adjustment of the hydroxy group contents of the polyvinyl
acetal X and the polyvinyl acetal Y allows control of the plasticizer contents in
the sound insulation layer and the protective layer, lowering the glass transition
temperature of the sound insulation layer. As a result, the sound-insulating properties
of the laminated glass are further improved. The plasticizer content (hereafter, also
referred to as content X) based on 100 parts by mass of the polyvinyl acetal X in
the sound insulation layer is preferably greater than the plasticizer content (hereafter,
also referred to as content Y) based on 100 parts by mass of the polyvinyl acetal
Y in the protective layer, more preferably greater by 5 parts by mass or more, still
more preferably greater by 15 parts by mass or more, particularly preferably greater
by 20 parts by mass or more because the sound-insulating properties of the laminated
glass is still further improved. Adjustment of the content X and the content Y lowers
the glass transition temperature of the sound insulation layer. As a result, the sound-insulating
properties of the laminated glass are still further improved.
[0098] The thickness of the protective layer is not limited as long as it is adjusted within
the range that allows the layer to serve as a protective layer. When the protective
layer has projections and recesses, the protective layer is preferably as thick as
possible in order to prevent transfer of the projections and recesses into the interface
between the protective layer and the sound insulation layer directly in contact with
the protective layer. Specifically, the lower limit of the thickness of the protective
layer is preferably 100 µm, more preferably 300 µm, still more preferably 400 µm,
particularly preferably 450 µm. The upper limit of the thickness of the protective
layer is not limited. In order to ensure the thickness enough to achieve sufficient
sound insulation properties, the upper limit is practically about 500 µm.
[0099] The sound insulating interlayer film may be produced by any method. For example,
sheets of the sound insulation layer and the protective layer are formed by a usual
sheet formation method such as an extrusion method, a calender method, or a press
method, and then these sheets are laminated.
[0100] The present invention also encompasses a laminated glass including the interlayer
film for laminated glass of the present invention interposed between a pair of glass
sheets.
[0101] The glass sheets may be commonly used transparent plate glass. Examples thereof include
inorganic glass such as float plate glass, polished plate glass, molded plate glass,
wired glass, wire-reinforced plate glass, colored plate glass, heat ray-absorbing
glass, heat ray-reflecting glass, and green glass. UV-shielding glass with a UV-shielding
coating layer on the surface may also be used. Further, organic plastic sheets such
as polyethylene terephthalate, polycarbonate, and polyacrylate sheets may also be
used.
[0102] Two or more different glass sheets may be used as the glass sheets. For example,
the interlayer film for laminated glass of the present invention may be interposed
between a transparent float plate glass and a colored plate glass such as green glass
to produce laminated glass. Two or more glass sheets different in thickness may be
used as the glass sheets.
- Advantageous Effects of Invention
[0103] The present invention can provide an embossed thermoplastic resin sheet that is capable
of enhancing deaeration during production of laminated glass and suppressing optical
distortion of the resulting laminated glass to improve the visibility when used as
an interlayer film for laminated glass, an engraved roll used for production of the
embossed thermoplastic resin sheet, a production method of the engraved roll, an interlayer
film for laminated glass including the embossed thermoplastic resin sheet, and a laminated
glass.
BRIEF DESCRIPTION OF DRAWINGS
[0104]
Fig. 1 is a schematic view for explaining the step of forming projections and recesses
in the method for producing an engraved roll of the present invention.
Fig. 2 is a schematic view for explaining the step of removing the blast material
in the method for producing an engraved roll of the present invention.
Fig. 3 is a schematic view for explaining the groove height, the width of a bottom
portion, the pitch interval and the angle of inclination of a recessed portion.
Fig. 4 shows a photo (a) of a recessed groove portion of an engraved roll photographed
after the step of forming projections and recesses in Example 1 and a photo (b) of
a recessed groove portion of the engraved roll photographed after the step of removing
the blast material in Example 1.
Fig. 5 shows a photo (a) of projections and recesses of an embossed thermoplastic
resin sheet obtained in Example 1 and a photo (b) of projections and recesses of an
embossed thermoplastic resin sheet obtained in Comparative Example 1.
Fig. 6 is an exemplary image data of an embossed thermoplastic resin sheet by a three-dimensional
profilometer.
DESCRIPTION OF EMBODIMENTS
[0105] Embodiments of the present invention are more specifically described in the following
with reference to, but not limited to, examples.
(Example 1)
(1) Preparation of raw material roll
[0106] A mirror-finished chilled iron roll (diameter: 600 mm) was prepared, and milled in
the circumferential direction for formation of a large number of recessed grooves
and projected ridges on the surface, while being rotated. A raw material roll was
thus prepared. In the milled pattern of projections and recesses on the raw material
roll, the groove height was 250 µm, the width of a bottom portion was 0 µm, the pitch
interval was 300 µm, the angle of inclination was 15°, and the axis angle of a recessed
groove was 85°.
(2) Production of engraved roll
[0107] The blast material used was alumina #250 (corresponding to #280 according to the
JIS standard (JIS R 6001-1998)). The blast material was sprayed to the raw material
roll at an angle of 0° relative to the line connecting the tip of a blast gun and
the axis of the raw material roll, while the raw material roll was rotated. In this
manner, an uneven pattern was formed on the surface of the raw material roll (Step
of forming projections and recesses).
[0108] The blast material was sprayed under the conditions of an air pressure of 2.5 kgf/cm
2, a nozzle aperture of 8 mm, and a rotation speed of the raw material roll of 30 m/min,
while the blast gun was moved from one end to the other end of the roll at a moving
speed of 2 mm per rotation of the raw material roll.
[0109] Then, the blast material was sprayed to the roll having the uneven pattern at an
angle of 0° relative to the tangential plane direction of the roll and in a direction
in parallel with the recessed grooves of the roll, while the roll is rotated, for
removal of the blast material remaining in the recessed grooves. In this manner, an
engraved roll was obtained (Step of removing blast materials).
(3) Production of embossed thermoplastic resin sheet
[0110] Polyvinyl alcohol having an average degree of polymerization of 1700 was acetalized
with n-butylaldehyde to prepare polyvinyl butyral (acetyl group content: 1 mol%, butyral
group content: 69 mol%, hydroxy group content: 30 mol%). To 100 parts by mass of the
polyvinyl butyral were added 40 parts by mass of triethyleneglycol-di-2-ethylhexanoate
(3GO) as a plasticizer. The mixture was sufficiently kneaded with a mixing roll to
prepare a resin composition. The obtained resin composition was extruded through an
extruder to give a thermoplastic resin sheet with a thickness of 760 µm.
[0111] A pair of rolls including the obtained engraved roll and a rubber roll having a JIS
hardness of 70 to 90 was used as a device for transferring an uneven pattern. The
obtained thermoplastic resin sheet was passed through the device for transferring
an uneven pattern, whereby projections and recesses were transferred to one surface
of the sheet. The transfer conditions employed here were a temperature of the thermoplastic
resin sheet of 70°C, a temperature of the rolls of 140°C, a linear velocity of 10
m/min, and a linear pressure of 1 to 300 kN/m. Subsequently, the same treatment was
performed to transfer projections and recesses to the other surface of the sheet under
the same conditions.
(Examples 2 to 9)
[0112] Engraved rolls were produced under the same conditions for spraying the blast material
and through the same step for removing the blast material as those in Example 1, except
that the raw material roll used in " (2) Production of engraved roll" and the angle
for spraying the blast material relative to the tangential plane in the step of removing
the blast material were changed as shown in Tables 1 and 2. Then, embossed thermoplastic
resin sheets were produced. In Examples 8 and 9, however, only the step of forming
projections and recesses was performed and the step of removing the blast material
was not performed.
(Comparative Example 1, 2)
[0113] Engraved rolls were produced under the same conditions for spraying the blast material
as those in Example 1, except that the raw material roll used in " (2) Production
of engraved roll" was changed as shown in Table 2 and that the step of removing the
blast material was not performed. Then embossed thermoplastic resin sheets were produced.
(Example 10)
(Production of embossed multilayer thermoplastic resin sheet)
(1) Preparation of resin composition for forming first resin layer (sound insulation
layer)
[0114] Polyvinyl alcohol having an average degree of polymerization of 2400 was acetalized
with n-butyraldehyde to prepare polyvinyl butyral (acetyl group content: 12 mol%,
butyral group content: 66 mol%, hydroxy group content: 22 mol%). To 100 parts by mass
of the polyvinyl butyral were added 60 parts by mass of triethylene glycol-di-2-ethylhexanoate
(3GO) as a plasticizer. The mixture was sufficiently kneaded with a mixing roll. Thus,
a resin composition for forming a first resin layer (sound insulation layer) was prepared.
(2) Preparation of resin composition for forming second resin layer (protective layer)
[0115] Polyvinyl alcohol having an average degree of polymerization of 1700 was acetalized
with n-butyraldehyde to prepare polyvinyl butyral (acetyl group content: 1 mol%, butyral
group content: 69 mol%, hydroxy group content: 30 mol%). To 100 parts by mass of the
polyvinyl butyral were added 40 parts by mass of triethylene glycol-di-2-ethylhexanoate
(3GO) as a plasticizer. The mixture was sufficiently kneaded with a mixing roll. Thus,
a resin composition for forming a second resin layer (protective layer) was prepared.
(3) Preparation of interlayer film for laminated glass
[0116] The resin composition for forming a first resin layer (sound insulation layer) and
the resin composition for forming a second resin layer (protective layer) were co-extruded
through a co-extruder to produce a multilayer thermoplastic resin sheet (thickness:
0.8 mm) in which a first resin layer (sound insulation layer) was interposed between
two second resin layers (protective layers). The first resin layer had a thickness
of 0.1 mm, and the second resin layers each had a thickness of 0. 35 mm. Hereafter,
the three layers may be called a second resin layer A, the first resin layer, and
a second resin layer B in the order of lamination in the thickness direction for identification
of two second resin layers.
[0117] A pair of rolls including the engraved roll obtained in Example 1 and a rubber roll
having a JIS hardness of 70 to 90 was used as a device for transferring an uneven
pattern. The obtained multilayer thermoplastic resin sheet was passed through the
device for transferring an uneven pattern, whereby projections and recesses were transferred
to one surface of the sheet. The transferring conditions employed here were a temperature
of the thermoplastic resin sheet of 70°C, a temperature of the rolls of 140°C, a linear
velocity of 10 m/min, and a linear pressure of 1 to 300 kN/m. Subsequently, the same
treatment was performed to transfer projections and recesses to the other surface
of the sheet under the same conditions.
(Examples 11 to 22)
[0118] Engraved rolls were produced under the same conditions for spraying the blast material
and through the same step for removing the blast material as those in Example 10,
except that the composition of polyvinyl butyral used in the first resin layer and
the second resin layer, the raw material roll used in " (2) Production of engraved
roll", and the angle for spraying the blast material relative to the tangential plane
in the step of removing the blast material were changed as shown in Tables 3 to 5.
Then, embossed thermoplastic resin sheets were produced. In Examples 17 and 18, however,
only the step of forming projections and recesses was performed and the step of removing
the blast material was not performed.
(Comparative Example 3, 4)
[0119] Engraved rolls were produced under the same conditions for spraying the blast material
as those in Example 10, except that the raw material roll used in " (2) Production
of engraved roll" was changed as shown in Table 4 and that the step of removing the
blast material was not performed. Then, embossed thermoplastic resin sheets were produced.
(Evaluation)
[0120] The engraved rolls and the embossed thermoplastic resin sheets obtained in the examples
and the comparative examples were evaluated by the following methods.
[0121] Tables 1 to 5 show the results.
(1) Measurement of the number of blast material pieces present in recessed grooves
of engraved roll
[0122] The recessed groove portion of each engraved roll were photographed at a 200x magnification
with a microscope ("Dino-Lite Pro2, model: DILITE80" produced by AnMo Electronics
corporation). The number of remaining blast material pieces with a maximum length
of 10 µm or larger present in a range of 1290 µm × 1024 µm in the obtained photograph
was counted. The number of remaining blast material pieces was similarly counted at
10 points on each of the positions at 1/4, 2/4, and 3/4 of the obtained engraved roll
from both ends in the width direction in such a manner that each field of view does
not overlap with each other. The arithmetic mean of the obtained values was taken
as the average number of the blast material pieces in the recessed grooves of the
engraved roll.
[0123] The number of blast material pieces was counted after the step of forming projections
and recesses and after the step of removing blast materials. In Examples 8, 9, 17,
and 18 and Comparative Examples 1 to 4, counting of the number of the blast material
pieces after the step of removing the blast material was omitted because the step
of removing blast material pieces was not performed and the number of the blast material
pieces was not changed.
[0124] Fig. 4(a) is a photograph of a recessed groove portion of the engraved roll after
the step of forming projections and recesses in Example 1. Fig. 4 (b) is a photograph
of the recessed groove portion of the engraved roll after the step of removing the
blast material in Example 1.
(2) Evaluation of pattern of projections and recesses on embossed thermoplastic resin
sheet
[0125] The surface roughness of the embossed thermoplastic resin sheet in a field of view
of 5 mm × 5 mm was measured with a three-dimensional profilometer ("KS-1100" produced
by KEYENCE CORPORATION, head: model "LT-9510VM") for evaluation of the projections
and recesses on the embossed thermoplastic resin sheet. In the obtained image data,
Ra of the apex portions of the projections and height difference r were measured in
a direction in parallel with the projections. The number of portions where r is higher
than Ra by 30 µm or more was counted as defects. Here, Ra refers to the arithmetic
mean roughness Ra specified in JIS B-0601(1994). Ra is a value calculated using "KS-Analyzer
Ver. 2.00", analysis software included with the three-dimensional profilometer, in
the line roughness measurement mode based on the roughness profile data obtained by
drawing a measuring line from one end to the other end of the field of view in a direction
in parallel with the direction in which the apex portions of the projections are continuous.
The height difference r is determined as follows. The obtained roughness profile is
divided at 500-µm intervals into plural sections starting from the upper side or the
left side of the field of view with which an apex portion of a projection is in contact.
The difference between the maximum height and the minimum height in each section is
taken as the height difference r. The height difference of all the projections present
in the field of view is determined by the same method. The correction conditions employed
for obtaining the roughness profile data are cut-off value of 2.5 mm, no height smoothing,
no tilt correction, and automatic range setting. The measurement conditions other
than the field of view are as follows: stage feed condition: continuous; scan direction:
bi-directional scanning; leading axis: X-axis; stage travel rate: 250.0 µm/s; axis
feed rate: 10000.0 µm/s; measuring pitch of X axis: 2.0 µm; and measuring pitch of
Y axis: 2.0 µm. The arithmetic mean is obtained by counting the number of defects
at four points at each of the positions of 1/4, 2/4, and 3/4 of a roll of the resulting
thermoplastic resin sheet from both ends in the width direction. The obtained value
was taken as the number of defects of the projections.
[0126] Fig. 5 (a) is a photograph of projections and recesses of the embossed thermoplastic
resin sheet obtained in Example 1. Fig. 5(b) is a photograph of projections and recesses
of the embossed thermoplastic resin sheet obtained in Comparative Example 1.
[0127] Fig. 6 shows exemplary image data of embossed thermoplastic resin sheet created by
the three-dimensional profilometer.
[0128] The roughness (Rz) of the recesses in the shape of engraved lines on one surface
of the obtained embossed thermoplastic resin sheet was measured by a method in conformity
with JIS B-0601 (1994). The measurement may be performed in a direction perpendicular
to the engraved lines at a cut-off value of 2.5 mm, a standard length of 2.5 mm, a
measurement length of 12.5 mm, a tip radius of a stylus of 2 µm, a tip angle of 60°,
and a measurement rate of 0.5 mm/s. The roughness on the other surface on the opposite
side of the above surface was the same, and therefore, Tables 1 to 5 only show the
values of Rz on one surface.
(3) Evaluation of deaeration properties
[0129] The obtained embossed thermoplastic resin sheet was used as an interlayer film for
laminated glass, and a laminated glass was produced by preliminary pressure bonding
through deaeration under reduced pressure, followed by final pressure bonding, as
described below.
(Preliminary pressure bonding)
[0130] The interlayer film for laminated glass was sandwiched between two clear glass sheets
(30 cm in length × 30 cm in width × 2.5 mm in thickness), and a portion protruding
therefrom was cut, thereby preparing a laminate. The obtained laminate was placed
in a rubber bag, which was connected to a vacuum suction device. The rubber bag was
held under a reduced pressure of -60 kPa (absolute pressure of 16 kPa) for 10 minutes
with heating so that the temperature (preliminary pressure bonding temperature) of
the laminate reached 70°C. Thereafter, the pressure was returned to atmospheric pressure,
whereby completing the preliminary pressure bonding. The preliminary pressure bonding
was performed under three different conditions of a deaeration start temperature of
40°C, 50°C, and 60°C.
(Final pressure bonding)
[0131] The laminate after the preliminary pressure bonding was placed in an autoclave and
held at a temperature of 140°C and a pressure of 1300 kPa for 10 minutes. Then, the
temperature was lowered to 50°C and the pressure was returned to atmospheric pressure,
whereby the final pressure bonding was completed. A laminated glass was thus prepared.
(Bake test of laminated glass)
[0132] The obtained laminated glass was heated in an oven at 140°C for two hours. The resulting
laminated glass was taken out from the oven and cooled for three hours. The appearance
of the laminated glass was visually observed to check the number of the laminated
glass sheets in which foaming (bubbles) occurred for evaluation of deaeration properties.
Twenty sheets were tested for each laminated glass.
[0133] The case where the number of glass sheets in which foaming occurred was 5 or less
among 20 sheets under any of the deaeration start temperature conditions was rated
"o (good)". The case where the number of glass sheets in which foaming occurred was
more than 5 among 20 sheets under any one of the deaeration start temperature conditions
was rated "x (poor)".
(4) Evaluation of optical distortion (Visual evaluation)
[0134] A laminated glass was produced in the same manner as in the case of the evaluation
of deaeration properties.
[0135] A fluorescent lamp (produced by Panasonic Corporation, FL32S.D) was set at a point
of 7 m distant from an observer. The laminated glass was set at a point of 40 cm distant
from the observer on the line connecting the fluorescent lamp and the observer in
such a manner that the laminated glass was inclined 45° relative to the horizontal
plane. The case where the fluorescent lamp seen through the laminated glass was distorted
was rated "x (poor)", and the case where the fluorescent lamp seen through the laminated
glass was not distorted was rated "o (good)". The optical distortion was evaluated
at 25°C.
(5) Evaluation of optical distortion value
[0136] A laminated glass was produced in the same manner as in the case of evaluation of
deaeration properties.
[0137] The optical distortion value was measured with an optical distortion inspecting device
disclosed in
JP-A H07-306152. The optical distortion inspecting device includes: a light source unit which emits
illumination light toward a light-transmitting object to be inspected; a projection
plane where the illumination light having passed through the object to be inspected
is projected; an image inputting section for generating a gradation image by capturing
the projection plane; and an image processing section for determining the presence
or absence of distortion based on the variation in the gradation level of the gradation
image generated by the image inputting section. Specifically, upon evaluation of the
optical distortion by using EYE DICHO-COOL HALOGEN (15V100W) produced by Iwasaki Electric
Co., Ltd. as a light source, the illuminance of the light source, the angle of a screen
where an optical distortion image is to be projected, and the angle of a camera were
adjusted in such a manner that a laminated glass including a single layer film having
a visible light transmittance in conformity with JIS R3211 (1988) (value for Y under
standard illuminant A, A-Y (380 to 780 nm)) of 88% ("U4100" produced by Hitachi High-Technologies
Corporation was used) had an optical distortion value of 1.14 and that the optical
distortion value in a state of including no glass was adjusted to 1.30. The optical
distortion was evaluated under the condition of the laminated glass temperature of
25°C. As the optical distortion values, values in the lengthwise direction and in
the width direction can be calculated. In the present case, the smaller value of the
two was employed as the optical distortion value. The thermometer used was a contact-type
thermometer.
[Table 1]
| |
Example 1 |
Example 2 |
Example 3 |
Example 4 |
Example 5 |
Example 6 |
| Shape of recessed grooves of raw material roll |
Groove height (µm) |
250 |
330 |
250 |
250 |
250 |
80 |
| Width of bottom portion (µm) |
0 |
15 |
40 |
40 |
40 |
5 |
| Pitch interval (µm) |
300 |
200 |
400 |
400 |
400 |
220 |
| Angle of inclination (°) |
15 |
15 |
15 |
15 |
15 |
15 |
| Roll diameter (mm) |
600 |
600 |
600 |
600 |
600 |
600 |
| Axis angle of recessed groove (°) |
85 |
85 |
85 |
85 |
85 |
85 |
| Step of removing blast material |
Spraying angle relative to tangential plane of roll (°) |
0 |
0 |
0 |
15 |
10 |
10 |
| Number of blast material pieces in recessed grooves of engraved roll (pcs/mm2) |
After step of forming projections and recesses |
80 |
100 or more |
60 |
60 |
60 |
100 or more |
| After step of removing blast material |
0.30 |
0.71 |
0.20 |
2.75 |
1.45 |
2.83 |
| Number of defective projections or recesses on embossed thermoplastic resin sheet
(pcs/mm2) |
0.04 |
0.08 |
0.02 |
0.25 |
0.15 |
0.77 |
| Roughness of embossment at apex portion |
Ra (µm) |
3.5 |
4.3 |
4.5 |
3.5 |
3 |
2.5 |
| Roughness of embossment |
Rz (µm) |
38 |
33 |
35 |
35 |
34 |
40 |
| Evaluation of deaeration properties |
Deaeration start temperature (°C) |
40 |
50 |
60 |
40 |
50 |
60 |
40 |
50 |
60 |
40 |
50 |
60 |
40 |
50 |
60 |
40 |
50 |
60 |
| Preliminary pressure bonding temperature (°C) |
70 |
70 |
70 |
70 |
70 |
70 |
70 |
70 |
70 |
70 |
70 |
70 |
70 |
70 |
70 |
70 |
70 |
70 |
| Bake test (Number of sheets with foaming/20 sheets) |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
1 |
0 |
1 |
3 |
0 |
1 |
1 |
1 |
1 |
1 |
| Evaluation |
○ |
○ |
○ |
○ |
○ |
○ |
[Table 2]
| |
Example 7 |
Example 8 |
Example 9 |
Comparative Example 1 |
Comparative Example 2 |
| Shape of recessed grooves of raw material roll |
Groove height (µm) |
80 |
200 |
200 |
250 |
250 |
| Width of bottom portion (µm) |
0 |
30 |
30 |
0 |
40 |
| Pitch interval (µm) |
190 |
300 |
300 |
300 |
400 |
| Angle of inclination (°) |
15 |
30 |
25 |
15 |
15 |
| Roll diameter (mm) |
600 |
600 |
600 |
600 |
600 |
| Axis angle of recessed groove (°) |
85 |
85 |
85 |
85 |
85 |
| Step of removing blast material |
Spraying angle relative to tangential plane of roll (°) |
0 |
- |
- |
0 |
0 |
| Number of blast material pieces present in recessed grooves of engraved roll (pcs/mm2) |
After step of forming projections and recesses |
100 or more |
11 |
24 |
80 |
60 |
| After step of removing blast material |
2.75 |
- |
- |
- |
- |
| Number of defective projections or recesses on embossed thermoplastic resin sheet
(pcs/mm2) |
0.90 |
1.15 |
2.73 |
12.00 |
6.00 |
| Roughness of embossment at apex portion |
Ra (µm) |
2.5 |
4.5 |
3.5 |
6 |
5.8 |
| Roughness of embossment |
Rz (µm) |
34 |
38 |
35 |
35 |
33 |
| Evaluation of deaeration properties |
Deaeration start temperature (°C) |
40 |
50 |
60 |
40 |
50 |
60 |
40 |
50 |
60 |
40 |
50 |
60 |
40 |
50 |
60 |
| Preliminary pressure bonding temperature (°C) |
70 |
70 |
70 |
70 |
70 |
70 |
70 |
70 |
70 |
70 |
70 |
70 |
70 |
70 |
70 |
| Bake test (Number of sheets with foaming/20 sheets) |
0 |
1 |
2 |
1 |
1 |
3 |
2 |
2 |
4 |
2 |
5 |
8 |
2 |
3 |
6 |
| Evaluation |
○ |
○ |
○ |
× |
× |
[Table 3]
| |
Example 10 |
Example 11 |
Example 12 |
Example 13 |
Example 14 |
Example 15 |
| Formulation |
Composition of protective layer |
Bu degree (mol%) |
69 |
69 |
69 |
69 |
69 |
69 |
| OH degree (mol%) |
30 |
30 |
30 |
30 |
30 |
30 |
| Ac degree (mol%) |
1 |
1 |
1 |
1 |
1 |
1 |
| Plasticizer content (phr) |
40 |
40 |
40 |
40 |
40 |
40 |
| Composition of sound-insutatine layer |
Bu degree (mol%) |
66 |
66 |
66 |
66 |
66 |
66 |
| OH degree (mol%) |
22 |
22 |
22 |
22 |
22 |
22 |
| Ac degree (mol%) |
12 |
12 |
12 |
12 |
12 |
12 |
| Plasticizer content (phr) |
60 |
60 |
60 |
60 |
60 |
60 |
| Thickness |
Second resin layer A (µm) |
350 |
350 |
350 |
350 |
350 |
350 |
| First resin layer (µm) |
100 |
100 |
100 |
100 |
100 |
100 |
| Second resin layer B(µm) |
350 |
350 |
350 |
350 |
350 |
350 |
| Shape of recessed grooves of raw material roll |
Groove height (µm) |
250 |
330 |
250 |
250 |
250 |
80 |
| Width of bottom portion (µm) |
0 |
15 |
40 |
40 |
40 |
5 |
| Pitch interval (µm) |
300 |
200 |
400 |
400 |
400 |
220 |
| Angle of inclination (°) |
15 |
15 |
15 |
15 |
15 |
15 |
| Roll diameter (mm) |
600 |
600 |
600 |
600 |
600 |
600 |
| Axis angle of recessed groove (°) |
85 |
85 |
85 |
85 |
85 |
85 |
| Step of removing blast material |
Spraying angle relative to tangential plane of roll (°) |
0 |
0 |
0 |
15 |
10 |
10 |
| Number of blast material pieces present in recessed grooves on engraved roll (pcs/mm2) |
After step of forming projections and recesses |
80 |
100 or more |
60 |
60 |
60 |
100 or more |
| After step of removing blast material |
0.30 |
0.71 |
0.20 |
2.75 |
1.45 |
2.83 |
| Number of defective projections or recesses on embossed thermoplastic resin sheet
(pcs/mm2) |
0.04 |
0.09 |
0.02 |
0.24 |
0.13 |
0.67 |
| Roughness of embossment at apex portion |
Ra (µm) |
2.3 |
2.5 |
3.5 |
2.5 |
2.4 |
3.5 |
| Roughness of embossment |
Rz (µm) |
33 |
35 |
34 |
35 |
33 |
40 |
| Evaluation of deaeration properties |
Deaeration start temperature (°C) |
40 |
50 |
60 |
40 |
50 |
60 |
40 |
50 |
60 |
40 |
50 |
60 |
40 |
50 |
60 |
40 |
50 |
60 |
| Preliminary pressure bonding temperature (°C) |
70 |
70 |
70 |
70 |
70 |
70 |
70 |
70 |
70 |
70 |
70 |
70 |
70 |
70 |
70 |
70 |
70 |
70 |
| Bake test (Number of sheets with foaming/20 sheets) |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
1 |
1 |
1 |
2 |
1 |
1 |
1 |
1 |
1 |
2 |
| Evaluation |
○ |
○ |
○ |
○ |
○ |
○ |
| Visual evaluation of optical distortion |
25°C |
○ |
○ |
○ |
○ |
○ |
○ |
| Optical distortion value |
25°C |
1.40 |
1.40 |
1.40 |
1.41 |
1.45 |
1.48 |
[Table 4]
| |
Example 16 |
Example 17 |
Example 18 |
Comparative Example 3 |
Comparative Example 4 |
| Formulation |
Composition of protective layer |
Bu degree (mol%) |
69 |
69 |
69 |
69 |
69 |
| OH degree (mol%) |
30 |
30 |
30 |
30 |
30 |
| Ac degree (mol%) |
1 |
1 |
1 |
1 |
1 |
| Plasticizer content (phr) |
40 |
40 |
40 |
40 |
40 |
| Composition of sound insulation layer |
Bu degree (mol%) |
66 |
66 |
66 |
66 |
66 |
| OH degree (mol%) |
22 |
22 |
22 |
22 |
22 |
| Ac degree (mol%) |
12 |
12 |
12 |
12 |
12 |
| Plasticize content (phr) |
60 |
60 |
60 |
60 |
60 |
| Thickness |
Second resin layer A (µm) |
350 |
350 |
350 |
350 |
350 |
| First resin layer (µm) |
100 |
100 |
100 |
100 |
100 |
| Second resin layer B (µm) |
350 |
350 |
350 |
350 |
350 |
| Shape of recessed grooves of raw material roll |
Groove height (µm) |
80 |
200 |
200 |
250 |
250 |
| Width of bottom portion (µm) |
0 |
30 |
30 |
0 |
40 |
| Pitch interval (µm) |
190 |
300 |
300 |
300 |
400 |
| Angle of inclination (°) |
15 |
30 |
25 |
15 |
15 |
| Roll diameter (mm) |
600 |
600 |
600 |
600 |
600 |
| Axis angle of recessed groove (°) |
85 |
85 |
85 |
85 |
85 |
| Step of removing blast material |
Spraying angle relative to tangential plane of roll (°) |
0 |
- |
- |
0 |
0 |
| Number of blast material pieces present in recessed grooves of engraved roll (pcs/mm2) |
After step of forming projections and recesses |
100 or more |
11 |
24 |
80 |
60 |
| After step of removing blast materials |
2.75 |
- |
- |
- |
- |
| Number of defective projections or recesses on embossed thermoplastic resin sheet
(pcs/mm2) |
0.97 |
1.35 |
2.70 |
11.50 |
6.50 |
| Roughness of embossment at apex portion |
Ra (µm) |
2.5 |
5.5 |
6.3 |
5.5 |
6.3 |
| Roughness of embossment |
Rz (µm) |
45 |
40 |
35 |
33 |
33 |
| Evaluation of deaeration properties |
Deaeration start temperature (°C) |
40 |
50 |
60 |
40 |
50 |
60 |
40 |
50 |
60 |
40 |
50 |
60 |
40 |
50 |
60 |
| Preliminary pressure bonding temperature (°C) |
70 |
70 |
70 |
70 |
70 |
70 |
70 |
70 |
70 |
70 |
70 |
70 |
70 |
70 |
70 |
| Bake test (Number of sheets with foaming/20 sheets) |
1 |
1 |
3 |
1 |
2 |
4 |
1 |
3 |
4 |
3 |
5 |
13 |
3 |
5 |
10 |
| Evaluation |
○ |
○ |
○ |
× |
× |
| Visual evaluation of optical distortion |
25°C |
○ |
○ |
○ |
× |
× |
| Optical distortion value |
25°C |
1.49 |
1.56 |
1.79 |
3.50 |
2.21 |
[Table 5]
| |
Example 19 |
Example 20 |
Example 21 |
Example 22 |
| Formulation |
Composition of protective layer |
Bu degree (mol%) |
69 |
68.5 |
69 |
70 |
| OH degree (mol%) |
30 |
31 |
30.7 |
29 |
| Ac degree (mol%) |
1 |
0.5 |
0.3 |
1 |
| Plasticizer content (phr) |
36 |
36 |
37.5 |
39 |
| Composition of sound insulation layer |
Bu degree (mol%) |
66 |
67.5 |
71 |
77.7 |
| OH degree (mol%) |
24.5 |
24.5 |
23 |
20.8 |
| Ac degree (mol%) |
10.5 |
8 |
6 |
1.5 |
| Plasticizer content (phr) |
75 |
75 |
76 |
77 |
| Thickness |
Second resin layer A (µm) |
350 |
350 |
350 |
350 |
| First resin layer (µm) |
100 |
100 |
100 |
100 |
| Second resin layer B(µm) |
350 |
350 |
350 |
350 |
| Shape of recessed grooves of raw material roll |
Groove height (µm) |
250 |
250 |
250 |
250 |
| Width of bottom portion (µm) |
0 |
0 |
0 |
0 |
| Pitch interval (µm) |
300 |
300 |
300 |
300 |
| Angle of inclination (°) |
15 |
15 |
15 |
15 |
| Roll diameter (mm) |
600 |
600 |
600 |
600 |
| Axis angle of recessed groove (°) |
85 |
85 |
85 |
85 |
| Step of removing blast material |
Spraying angle relative to tangential plane of roll (°) |
0 |
0 |
0 |
0 |
| Number of blast material pieces present in recessed grooves on engraved roll (pcs/mm2) |
After step of forming projections and recesses |
80 |
80 |
80 |
80 |
| After step of removing blast materials |
0.30 |
0.30 |
0.30 |
0.30 |
| Number of defective projections or recesses on embossed thermoplastic resin sheet
(pcs/mm2) |
0.03 |
0.01 |
0.03 |
0.02 |
| Roughness of embossment at apex portion |
Ra (µm) |
3.2 |
3.3 |
2.5 |
2.6 |
| Roughness of embossment |
Rz (µm) |
37 |
38 |
40 |
40 |
| Evaluation of deaeration properties |
Deaeration start temperature (°C) |
40 |
50 |
60 |
40 |
50 |
60 |
40 |
50 |
60 |
40 |
50 |
60 |
| Preliminary pressure bonding temperature (°C) |
70 |
70 |
70 |
70 |
70 |
70 |
70 |
70 |
70 |
70 |
70 |
70 |
| Bake test (Number of sheets with foaming/20 sheets) |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Evaluation |
○ |
○ |
○ |
○ |
| Visual evaluation of optical distortion |
25°C |
○ |
○ |
○ |
○ |
| Optical distortion value |
25°C |
1.36 |
1.39 |
1.41 |
1.38 |
INDUSTRIAL APPLICABILITY
[0138] The present invention can provide an embossed thermoplastic resin sheet that is capable
of enhancing deaeration during production of laminated glass and suppressing optical
distortion of the resulting laminated glass to improve the visibility when used as
an interlayer film for laminated glass, an engraved roll used for production of the
embossed thermoplastic resin sheet, a production method of the engraved roll, an interlayer
film for laminated glass including the embossed thermoplastic resin sheet, and a laminated
glass.
REFERENCE SIGNS LIST
[0139]
- 1.
- Roll
- 2.
- Blast gun